Emergent Management of Gonorrhea

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Overview

In emergency department (ED) patients who clinical presentation suggests gonorrhea, specimens from likely sites of infection should be sent to the laboratory to be cultured for N gonorrhoeae and Chlamydia species. Nucleic acid amplification tests (NAATs) may be used in addition to or in place of culture depending on availability and laboratory preferences.[1] The possibility of other sexually transmitted diseases (STDs) should be evaluated.

Begin appropriate antibiotic therapy for gonorrhea as soon as possible. Chlamydial infection is found frequently in patients with gonorrhea; thus, empiric antibiotic therapy should always provide coverage for both infections in any patients other than newborns. Gonococcal infection in HIV-positive patients is treated with the same regimen used for the general population.

Pain relief may be needed for patients with epididymitis, pelvic inflammatory disease, and disseminated gonococcal infection (DGI). Aspiration of purulent joint effusions may improve the patient’s comfort and recovery.

Partner diagnosis and treatment is important to prevent reinfection and complications. Counsel patients to abstain from sexual activity until after full treatment and testing and treatment of partners is complete. Patients should receive information and counseling to help them avoid future STDs and unwanted pregnancies.

Social services should be consulted immediately in cases of suspected sexual assault, child abuse, or elder abuse. Clinicians should be aware, however, that gonorrhea can be transmitted to children nonsexually (eg, spread of infection can occur via contaminated hands of infected caregivers).[2]

For more information, see the Medscape Reference topic Gonorrhea.

Consultations

Consult a gynecologist for patients with severe pelvic inflammatory disease and for any pregnant patient with a sexually transmitted infection (STD). Consult a pediatrician for any child with an STD.

Consult an ophthalmologist for every patient with gonococcal conjunctivitis (see image below). This disease may progress rapidly and can cause permanent loss of vision.



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Patient presented with gonococcal urethritis, which became systemically disseminated, leading to gonococcal conjunctivitis of the right eye. Courtesy ....

Antibiotic Treatment

Because of resistance with oral cephalosporins, only 1 regimen, dual treatment with ceftriaxone IM and azithromycin PO, is recommended for treatment of gonorrhea in the United States. Dual therapy with ceftriaxone and azithromycin should be administered together on the same day, preferably simultaneously and under direct observation. In addition, persons infected with N gonorrhoeae frequently are coinfected with C trachomatis; this finding has led to the longstanding recommendation that persons treated for gonococcal infection also be treated with a regimen that is effective against uncomplicated genital C trachomatis infection, further supporting the use of dual therapy that includes azithromycin.[3]

Because of the persistent increase in multidrug-resistant gonorrhea, the CDC 2015 recommendations' preferred dual-drug regimen consists of the following:[4]

The 250-mg IM dose of ceftriaxone is recommended over the 125-mg dose, given concern for resistance, prior lower-dose ceftriaxone dose failures, and seemingly improved efficacy in pharyngeal infections. Ceftriaxone is safe and effective in pregnant women and probably destroys incubating syphilis. Its major drawback is the necessity for IM administration.

Since 2007, the Centers for Disease Control and Prevention (CDC) has not recommended fluoroquinolone antibiotics for the treatment of gonorrhea in the United States because of bacterial resistance.

In August 2012, the CDC announced changes to 2010 sexually transmitted disease guidelines for gonorrhea treatment. The Gonococcal Isolate Surveillance Project (GISP) described a decline in cefixime susceptibility among urethral N gonorrhoeae isolates in the United States during 2006-2011. Because of cefixime’s lower susceptibility, new guidelines were issued that no longer recommend oral cephalosporins for first-line gonococcal infection treatment.[5]

Alternate treatment options

If ceftriaxone is unavailable, patients can be given a single dose of cefixime 400 mg PO plus a single dose of azithromycin 1 g PO.

If cephalosporin allergic, consider alternant dual therapy with single doses of gemifloxacin PO 320 mg plus azithromycin 2 g PO, or gentamicin 240 mg IM plus azithromycin 2 g PO.

Another alternative regimen for patients intolerant of cephalosporins is spectinomycin (2 g IM). Spectinomycin may be costly and is currently unavailable in the United States.

If azithromycin allergic, doxycycline (100 mg PO BID for 7 days) can be used in place of azithromycin as an alternative second antimicrobial when used in combination with ceftriaxone (preferably) or cefixime.

Drug resistance

Although cephalosporins remain an effective treatment for gonococcal infections, the CDC has reported that resistance to cefixime increased from 0.2% in 2000 to 1.4% in 2010 and back down to 0.4% in 2013, and resistance to ceftriaxone increased from less than 0.1% to 0.4% in 2011 and back down to 0.05% in 2013.[4] However, the reported rates of resistance to ceftriaxone have been much higher in countries such as Japan, Spain, and France.[4] Oral cephalosporins are no longer recommended as first-line treatment for gonorrhea because of increasing resistance. Additionally, a high prevalence of tetracycline resistance among GISP isolates was observed, particularly among patients with elevated MICs to cefixime.[5]

Spectinomycin

Spectinomycin (Trobicin) is indicated for patients with beta-lactam intolerance. It is a second-line choice due to poor efficacy in pharyngitis. This drug is currently unavailable in the United States.

Gentamicin

A review of the literature identified trials using single-dose gentamicin, an aminoglycoside, in the treatment of uncomplicated gonococcal infections in patients older than 16 years owing to the increase in antibiotic resistance. Although the primary outcome was the microbiological cure of N gonorrhoeae infection, further randomized trials are indicated.[6]

For more information see, CDC Sexually Transmitted Diseases Treatment Guidelines, 2015.

Hospital Admission

Hospitalization is recommended for initial treatment of disseminated gonococcal infection (especially for patients who are unlikely to return for follow-up doses of antibiotics), purulent joint infections, meningitis, and endocarditis.[4]

Hospitalization is recommended for initial treatment of pelvic inflammatory disease (PID) cases in the presence of the following factors:

Further Outpatient Care

Patients with disseminated gonococcal infection or pelvic inflammatory disease who are treated on an outpatient basis must receive follow-up care within 72 hours. Early follow-up care and culture with antibiotic sensitivities is indicated for patients with unresolved or recurrent symptoms.

Follow-up for test of cure is indicated for all pharyngitis cases treated with spectinomycin, as its efficacy is less than 60%.

Recurrent symptoms may result from re-infection rather than treatment failure. However, if treatment failure is suspected, culture of isolates is recommended.[4]

Instruct patients with uncomplicated cases to follow up with a primary care or public health provider to reduce the risk of future infection.

Deterrence/Prevention

All patients with gonococcal infection should refer all their sex partners (whether symptomatic or asymptomatic) for evaluation and treatment.

All infants born to mothers with untreated gonococcal infection should be treated prophylactically with a single dose of ceftriaxone 25-50 mg/kg IV or IM, not to exceed 125 mg. All neonates should undergo prophylaxis for ophthalmia neonatorum with silver nitrate (1%) aqueous solution OU once or erythromycin (0.5%) ophthalmic ointment OU once.

Condoms offer partial protection against gonococcal infection and should be recommended.[7]

Author

Bruce M Lo, MD, MBA, CPE, RDMS, FACEP, FAAEM, FACHE, Chief, Department of Emergency Medicine, Sentara Norfolk General Hospital; Medical Ditector, Sentara Transfer Center; Professor and Assistant Program Director, Core Academic Faculty, Department of Emergency Medicine, Eastern Virginia Medical School

Disclosure: Nothing to disclose.

Specialty Editors

Francisco Talavera, PharmD, PhD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

Barry J Sheridan, DO, Chief Warrior in Transition Services, Brooke Army Medical Center

Disclosure: Nothing to disclose.

Chief Editor

Steven C Dronen, MD, FAAEM, Chair, Department of Emergency Medicine, LeConte Medical Center

Disclosure: Nothing to disclose.

Additional Contributors

Amy J Behrman, MD, Associate Professor, Department of Emergency Medicine, Director, Division of Occupational Medicine, Perelman School of Medicine at the University of Pennsylvania

Disclosure: Nothing to disclose.

Edward A Michelson, MD, Associate Professor, Program Director, Department of Emergency Medicine, University Hospital Health Systems of Cleveland

Disclosure: Nothing to disclose.

Acknowledgements

Catherine T Shoff, DO Staff Physician, Departments of Pulmonary, Critical Care and Sleep Medicine, Director, Tri-Services Adult Cystic Fibrosis Center, Wilford Hall Medical Center; Assistant Professor of Medicine, Uniformed Services University of the Health Sciences

Catherine T Shoff, DO is a member of the following medical societies: American Academy of Sleep Medicine and American College of Chest Physicians

Disclosure: Nothing to disclose.

References

  1. Whiley DM, Tapsall JW, Sloots TP. Nucleic acid amplification testing for Neisseria gonorrhoeae: an ongoing challenge. J Mol Diagn. 2006 Feb. 8(1):3-15. [View Abstract]
  2. Goodyear-Smith F. What is the evidence for non-sexual transmission of gonorrhoea in children after the neonatal period? A systematic review. J Forensic Leg Med. 2007 Nov. 14(8):489-502. [View Abstract]
  3. Workowski KA, Bolan GA. Sexually transmitted diseases treatment guidelines, 2015. MMWR Recomm Rep. 2015 Jun 5. 64 (RR-03):1-137. [View Abstract]
  4. Centers for Disease Control and Prevention. Gonococcal Infections. Centers for Disease Control and Prevention. Available at http://www.cdc.gov/std/tg2015/gonorrhea.htm. June 4, 2015; Accessed: March 23, 2016.
  5. Update to CDC's Sexually Transmitted Diseases Treatment Guidelines, 2010: Oral Cephalosporins No Longer a Recommended Treatment for Gonococcal Infections. MMWR Morb Mortal Wkly Rep. 2012 Aug 10. 61:590-4. [View Abstract]
  6. Hathorn E, Dhasmana D, Duley L, Ross JD. The effectiveness of gentamicin in the treatment of Neisseria gonorrhoeae: a systematic review. Syst Rev. 2014 Sep 19. 3(1):104. [View Abstract]
  7. Warner L, Stone KM, Macaluso M, Buehler JW, Austin HD. Condom use and risk of gonorrhea and Chlamydia: a systematic review of design and measurement factors assessed in epidemiologic studies. Sex Transm Dis. 2006 Jan. 33(1):36-51. [View Abstract]
  8. Cephalosporin Susceptibility Among Neisseria gonorrhoeae Isolates --- United States, 2000--2010. MMWR Morb Mortal Wkly Rep. 2011 Jul 8. 60(26):873-7. [View Abstract]
  9. [Guideline] Centers for Disease Control and Prevention. Update to CDC's sexually transmitted diseases treatment guidelines, 2006: fluoroquinolones no longer recommended for treatment of gonococcal infections. MMWR Morb Mortal Wkly Rep. 2007 Apr 13. 56(14):332-6. [View Abstract]
  10. Golden MR, Barbee LA, Kerani R, Dombrowski JC. Potential Deleterious Effects of Promoting the Use of Ceftriaxone in the Treatment of Neisseria gonorrhoeae. Sex Transm Dis. 2014 Oct. 41(10):619-25. [View Abstract]
  11. Golparian D, Ohlsson A, Janson H, Lidbrink P, Richtner T, Ekelund O, et al. Four treatment failures of pharyngeal gonorrhoea with ceftriaxone (500 mg) or cefotaxime (500 mg), Sweden, 2013 and 2014. Euro Surveill. 2014 Jul 31. 19(30):[View Abstract]
  12. Availability of cefixime 400 mg tablets--United States, April 2008. MMWR Morb Mortal Wkly Rep. 2008 Apr 25. 57(16):435. [View Abstract]
  13. Centers for Disease Control and Prevention. 2009 Sexually transmitted diseases surveillance: gonorrhea. Available at http://www.cdc.gov/STD/stats09/gonorrhea.htm. Accessed: 5/27/11.

Patient presented with gonococcal urethritis, which became systemically disseminated, leading to gonococcal conjunctivitis of the right eye. Courtesy of the CDC/Joe Miller, VD

Patient presented with gonococcal urethritis, which became systemically disseminated, leading to gonococcal conjunctivitis of the right eye. Courtesy of the CDC/Joe Miller, VD

Patient presented with gonococcal urethritis, which became systemically disseminated, leading to gonococcal conjunctivitis of the right eye. Courtesy of the CDC/Joe Miller, VD